trimethylsilyl N-trimethylsilylethanimidate

HCID 25248CAS 10416-59-8

Basic information

Standard SMILES
CC(=N[Si](C)(C)C)O[Si](C)(C)C
InChIKey
SIOVKLKJSOKLIF-UHFFFAOYSA-N
Molecular formula
C8H21NOSi2
Average molar mass
203.43 g/mol
Monoisotopic mass
203.11616735

Names & identifiers

Preferred name
trimethylsilyl N-trimethylsilylethanimidate
IUPAC
trimethylsilyl N-trimethylsilylethanimidate
English name
N,O-Bis(trimethylsilyl)acetamide
Molecular formula
C8H21NOSi2
Molecular weight
203.43

Names & synonyms

trimethylsilyl N-trimethylsilylethanimidateC8H21NOSi2n,o-bis(trimethylsilyl) acetamideTMS-BATRIMETHYLSILYL N-(TRIMETHYLSILYL)ACETIMIDATEDynasylan BSAtrimethylsilyl (E)-N-(trimethylsilyl)acetimidateTRIMETHYLSILYL N-(TRIMETHYLSILYL)ETHANIMIDATEBSA(E)-trimethylsilyl N-(trimethylsilyl)acetimidate132255-83-5Trimethylsilyl N-(trimethylsilyl)ethanimidoate
Show more names
BIS(TRIMETHYLSILYL)ACETAMIDECB2500bis(trimethylsllyl)acetamideN.O-Bis(trimethylsilyl)acetamide (BSA)
N,O-bis-(TRIMETHYLSILYL)-ACETAMIDEtrimethylsilyl (1E)-N-trimethylsilylethanimidateEzetimibe Impurity 168SCHEMBL682640SCHEMBL1301719SCHEMBL1301721N,O-bis(trimethlsilyl)acetamiden,o-bis (trimethylsilyl)acetamide

Database identifiers

CAS
10416-59-8
PubChem CID
25248
DTXSID
DTXSID5051525

Properties

Computed structural properties

Topological polar surface area
21.6 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
2
Rotatable bonds
3
Heavy atoms
12

Experimental & physicochemical properties

SpringerMaterials Properties29Si nuclear magnetic resonance spectrum

Physicochemical properties

Melting point
24 °C · 24 °C
Boiling point
71 · 71-73 °C35 mm Hg(lit.)
Density
0.832 g/mL · 0.832 g/mL at 20 °C(lit.)
vapor pressure
10 hPa · 10 hPa (50 °C)
refractive index
20 · n20/D 1.417(lit.)
Flash point
53 °F · 53 °F

Safety & regulation

Safety data

F
10-21
PPE
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
wgk
3
tsca
TSCA listed
rtecs
AK3000000
ridadr
UN 2920 8/PG 2

Chemistry & industry

Applications · 6 items

DescriptionClear to yellowish clear liquid liquid which is soluble in many nonpolar and polar aprotic solvents. The trimethylsilyl group is a frequently utilized monofunctional blocking group for protic organic and inorganic materials. As it eliminated during the silylation is neutral acetamide, N,O-Bis(trimethylsilyl)acetamide can be preferably used for substrates which are acid- or base-sensitive. N,O-bis(trimethylsilyl)-acetamide is an effective silylating agent. It is used in the pharmaceutical and in the chemical industry. Typically the silylating reaction with BSA results in neutral by-products only.

UsesUsed for blocking and protection of hydroxyl groups in natural products, e.g. amino acids, carbohydrates; Used for blocking and protection of functional groups in organic intermediates; Used for formation of derivatives of H-acid compounds for analysis; The silylated derivatives are volatile and can therefore be determined by gas chromatography. Deblocking is preferably carried out by means of hydrolysis, giving high yields. In some cases, thermal elimination of the trimethylsilyl group is possible.

UsesPowerful silylation reagent for a wide range of functional groups under mild conditions

UsesN,O-bis(trimethylsilyl)-acetamide (BSA) is frequently used with TMCS as a catalyst to modify a variety of functional groups including carboxyl groups. In one novel application, BSA was used to measure carboxypeptidase activity by forming derivatives which could be determined by gas chromatography.BSA has been used to prepare derivatives of steroids and glucocorticoids.

UsesN,O-Bis(trimethylsilyl)acetamide is a powerful silylating agent; reacts with a wide range of functional groups.BSA was used to trimethylsilylate the hydroxyl group of 12 selectively to form in almost quantitative yield (eq 32).The presence of catalytic amounts (~0.02 equiv) of tetrabutylammonium fluoride (TBAF) significantly promoted the silylation of alcohols under mild conditions with high chemoselectivity, i.e., TBAF plays a role as a smooth silyl transfer catalyst from nitrogen to the hydroxyl group.

General DescriptionN,O-Bis(trimethylsilyl)acetamide is an excellent silylation reagent. For some sterically hindered primary or secondary nitro compounds, N,O-bis(trimethylsilyl)acetamide and BSTFA achieve better results than normal silylation conditions.

Preparation methods

PreparationN,O-Bis(trimethylsilyl)acetamide is made by the reaction of acetamide with a large excess of chlorotrimethylsilane in the presence of triethylamine.

Suppliers50 total

梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
衢州润东化工有限公司0570-8789886 18892685668 · [email protected]
艾斯提克(山东)生物医药有限公司21-58999881 15623240527 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
爱斯特(成都)生物制药股份有限公司+86-28-85122536 85324413 · [email protected]

Related reactions

6 records

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